EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Eluting Coronary Stent Coronary Stents, Performance, and Technique in Chronic Total Occlusions
Completed · Not applicable
Conditions studied: Coronary Artery Disease (CAD), Chronic Total Occlusion (CTO)
In brief
A prospective, multi-center, single-arm study to establish the safety and effectiveness of the XIENCE V® Everolimus Eluting Coronary Stent, XIENCE nano™ Everolimus Eluting Coronary Stent, XIENCE PRIME™ LL Everolimus Eluting Coronary Stent, HT PROGRESS and HT PILOT Coronary Guide Wires, and MINI-TREK Coronary Dilatation Catheter in patients undergoing elective percutaneous revascularization of native chronic total coronary occlusions
Key facts
- Study ID
- NCT01435031
- Run by
- Abbott Medical Devices
- People needed
- 250
- Starts
- 2011-09-01
- Expected to finish
- 2017-12-01
- Last updated by the study team
- 2018-05-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Abbott Vascular — Santa Clara, California, United States
Full record on ClinicalTrials.gov
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